Meijer Severe Menthol Throat Drops

Manufacturer
Meijer | Bestco
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:26:44

Label at a glance#

ProductMeijer Severe Menthol Throat Drops
Active ingredientMENTHOL
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each drop)

Menthol 20 mg

OTC - PURPOSE SECTION

Purpose

Oral anesthetic

INDICATIONS & USAGE SECTION

Uses temporarily relieves:

  • occasional minor iritation and pain associated with sore throat and sore mouth

WARNINGS SECTION

Warnings

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a severe sore throat accompanied by difficulty in breathing or that lasts more than 2 days.
  • a sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting.

OTC - STOP USE SECTION

Stop use and consult doctor if

  • sore mouth does not improve in 7 days
  • irritation, pain or redness persists or worsens

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - WHEN USING SECTION

Do not exceed recommended dosage.

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children 12 years and over - dissolve 1 drop slowly in mouth. Repeat every two hours as needed or as directed by a doctor.

children 12 years and under - do not use

OTHER SAFETY INFORMATION

Other information

  • 10 calories per drop
  • do not use if bag is torn or open

INACTIVE INGREDIENT SECTION

Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C blue no. 1, glycerin, gum arabic, medium chain triglycerides, potassium sorbate, soybean oil, sucrose and water.

OTC - QUESTIONS SECTION

Questions? Or to report an adverse event call 1-800-245-2898, Monday - Friday, 9AM to 4PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Meijer Severe Menthol 45ct Throat DropMeijer Severe Menthol 45ct Throat Drop

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1995300menthol 20 MG Oral LozengePSN3
1995300menthol 20 MG Oral LozengeSCD3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130713733806268GTIN-13: 0713733806268
EAN-13: 0713733806268
GTIN-12: 713733806268
UPC-A: 713733806268
GTIN storage (14 digits): 00713733806268
Meijer Severe Menthol 45ct Throat Drop PN60002410.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0092-1Meijer Severe Menthol Throat Drops45 in 1 BAGLOZENGE453

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-009279481-0092-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Meijer Severe Menthol Throat DropsMENTHOLMeijer16603ca4-1ce5-2e7e-e063-6394a90ad6f12025-12-18WarningsExact identifier
ndc (package): 79481-0092-1
ndc (product): 79481-0092
ndc11 (package): 79481009201
spl id: 46410c0e-07e5-7194-e063-6394a90a3997
spl set id: 16603ca4-1ce5-2e7e-e063-6394a90ad6f1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.